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Plasma NT1‐tau and Aβ42 correlate with age and cognitive function in two large Down syndrome cohorts
- Stern, Andrew M;
- Van Pelt, Kathryn L;
- Liu, Lei;
- Anderson, Amirah K;
- Ostaszewski, Beth;
- Mapstone, Mark;
- O'Bryant, Sid;
- Petersen, Melissa E;
- Christian, Bradley T;
- Handen, Benjamin L;
- Selkoe, Dennis J;
- Schmitt, Frederick;
- Head, Elizabeth;
- investigators, the Alzheimer's Biomarker Consortium–Down Syndrome
- et al.
Published Web Location
https://doi.org/10.1002/alz.13382Abstract
Introduction
People with Down syndrome (DS) often develop Alzheimer's disease (AD). Here, we asked whether ultrasensitive plasma immunoassays for a tau N-terminal fragment (NT1-tau) and Aβ isoforms predict cognitive impairment.Methods
Plasma NT1-tau, Aβ37 , Aβ40 , and Aβ42 levels were measured in a longitudinal discovery cohort (N = 85 participants, 220 samples) and a cross-sectional validation cohort (N = 239). We developed linear models and predicted values in the validation cohort.Results
Discovery cohort linear mixed models for NT1-tau, Aβ42 , and Aβ37:42 were significant for age; there was no main effect of time. In cross-sectional models, NT1-tau increased and Aβ42 decreased with age. NT1-tau predicted cognitive and functional scores. The discovery cohort linear model for NT1-tau predicted levels in the validation cohort.Discussion
NT1-tau correlates with age and worse cognition in DS. Further validation of NT1-tau and other plasma biomarkers of AD neuropathology in DS cohorts is important for clinical utility.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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